Supharm recruited the experienced professional team (pharmacists, doctors, medical nurse .etc). They worked for the R.A. field for several years. With their professional knowledge and experiences, Supharm is confident to shorten the time needed for the license approval.
Supharm Provides the professional consultancy regulatory affairs service on the product license approval and the clinical trial for the industry of the pharmaceutical preparations, medical device…etc. With experiences, Supharm understands the clients’ needs. Supharm developed the flexible professional service on the contract based. At any times or stages needs for clients, we can commit for client’s requirement on the regulatory affairs service via provide consulting service for the large /or small scale project.